戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します
1                                      Crigler Najjar type 1 is a rare autosomal recessive condition ca
2                                      Crigler-Najjar syndrome (CN) is a very rare genetic disorder cha
3                                      Crigler-Najjar syndrome is a recessively inherited disorder char
4                                      Crigler-Najjar syndrome type 1 (CN-1) is a recessively inherited
5                                      Crigler-Najjar syndrome type I is characterized by unconjugated
6 in the UGT1A1 (HUG-Br1) isozyme of a Crigler-Najjar (CN) Type I patient.
7                      The Gunn rat, a Crigler-Najjar syndrome model animal lacking UDP-glucuronosyltra
8 c bilirubin glucuronidation, causing Crigler-Najjar syndrome type 1 or 2, respectively.
9                         In contrast, Crigler-Najjar syndrome types I and II are rare genetic disorder
10 he risk of bilirubin encephalopathy (Crigler-Najjar syndrome).
11                                  For Crigler-Najjar syndrome, an inherited disorder that results in f
12 cult, is now accepted management for Crigler-Najjar type I disease but remains controversial for the
13 rubinemia in humans that suffer from Crigler-Najjar type I disease results from lesions in the UGT1A1
14 r type II patients and, recently, in Crigler-Najjar type I patients treated with human hepatocyte cel
15                                   In Crigler-Najjar type II patients and, recently, in Crigler-Najjar
16 lirubinemia in the Gunn rat model of Crigler-Najjar syndrome can be achieved with one injection of HD
17 perbilirubinemic Gunn rats (model of Crigler-Najjar syndrome type 1) resulted in hUGT1A1 expression i
18 transplantation in the management of Crigler-Najjar syndrome, type 1.
19  rat is an excellent animal model of Crigler-Najjar syndrome, type 1.
20 hysiology, treatment, and outcome of Crigler-Najjar type 1 syndrome (CN1) in 28 UGT1A1 c.222C>A homoz
21  with urea cycle disorders (UCDs) or Crigler-Najjar (CN) syndrome 6 months posttransplantation.
22                    Patients with the Crigler-Najjar syndrome lack the enzyme uridine diphosphoglucuro
23 encoding UGT1A1 in patients with the Crigler-Najjar syndrome that was being treated with phototherapy
24  both alleles, whereas patients with Crigler-Najjar syndrome are homozygous for a defect that yields
25  report describes a young adult with Crigler-Najjar syndrome type II in whom kernicterus developed af
26 nduced levels noted in patients with Crigler-Najjar type 1 disease, is fatal in neonatal Ugt1(-/-) mi
27 s (n = 3), and patients (n = 4) with Crigler-Najjar type I (CN-I) syndrome.